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Phyllanthus maderaspatensis, a dietary supplement for the amelioration of adriamycin-induced toxicity and oxidative stress in mice

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Abstract

The effect of ethanol extract of Phyllanthus maderaspatensis (PME), a popular south Indian dietary supplement, was studied for its chemoprotective property on adriamycin (ADR)-induced toxicity and oxidative stress in mice. Adriamycin toxicity was evaluated biochemically by measuring the serum concentration of lactate dehydrogenase (LDH) and creatinine phosphokinase (CPK). Genotoxicity was evaluated by measuring the frequency of micronucleated polychromatic erythrocytes (MNPCEs) in bone marrow cells. Oxidative stress in the heart tissue was estimated by measuring the glutathione (GSH) levels in the homogenate. The treatment of mice with different doses of PME (400 mg/kg and 600 mg/kg body weight, p.o.,) for 7 days before the administration of a single i.p. dose of ADR (15 mg/kg) exhibited significant protection in a dose-dependent manner. The results clearly indicate that PME has a protective effect against ADR-induced toxicity, as revealed by the decrease in the concentrations of LDH, CPK, and the frequency of MNPCEs. The increased levels of GSH are indicative of the antioxidant property of PME.

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References

  1. Weijl NI, Cleton FJ, Osanto S (1997) Free radicals and antioxidants in chemotherapy-induced toxicity. Cancer Treat Rev 23:209–240

    Article  PubMed  CAS  Google Scholar 

  2. Thyagarajan SP, Subramanian S, Thirunalasundari T, Venkateswaran PS, Blumberg BS (1988) Effect of Phyllanthus amarus on chronic carriers of hepatitis B virus. Lancet 2:764–766

    Article  PubMed  CAS  Google Scholar 

  3. Unander DW, Venkateswaran PS, Millman I, Bryan HH, Blumberg BS (1990) Phyllanthus species: source of new antiviral compounds. In: Janick J, Simon JE (eds) Advances in new crops. Timber Press, Portland, Oregon, pp 518–521

    Google Scholar 

  4. Unander DW, Webster GL, Blumberg BS (1995) Usage and bioassays in Phyllanthus (Euphorbiaceae). IV. Clustering of antiviral uses and other effects. J Ethnopharmacol 45:1–18

    Article  PubMed  CAS  Google Scholar 

  5. Kirthikar KR, Basu BD (1999) In: Blatter E, Calus JF, Mhaskar KS (eds) Indian medicinal plants. International book distributors. Dehradun, India, pp 2222–2223

  6. Asha VV, Pushpangadan P (1998) Preliminary evaluation of the antihepatotoxic activity of Phyllanthus kozhikodianus, P. maderaspatensis and Solanum indicum. Fitoterapia 69:255–259

    Google Scholar 

  7. Asha VV, Akhila S, Wills PJ, Subramoniam A (2004) Further studies on the antihepatotoxic activity of Phyllanthus maderaspatensis Linn. J Ethnopharmacol 92:67–70

    Article  PubMed  CAS  Google Scholar 

  8. International Agency for Research on Cancer (IARC) (1987) IARC monographs on the evaluation of carcinogenic risks to human, vol 42. IARC, Lyon, France

  9. Sorsa M, Hemminki K, Vainio H (1985) Occupational exposure to anticancer drugs—potential and real hazards. Mutat Res 154:135–149

    PubMed  CAS  Google Scholar 

  10. Gewirtz DA (1999) A critical evaluation of the mechanisms of action proposed for the antitumor effects of the anthracycline antibiotics adriamycin and daunorubicin. Biochem Pharmacol 57:727–741

    Article  PubMed  CAS  Google Scholar 

  11. Gruber BM, Anuszewska EL, Skierski JS (2001) Activation of programmed cell death (apoptosis) by adriamycin in human neoplastic cells. Mutat Res 484:87–93

    PubMed  CAS  Google Scholar 

  12. Myers CE, McGuire WP, Liss RH, Ifrim I, Grotzinger K, Young RC (1977) Adriamycin: the role of lipid peroxidation in cardiac toxicity and tumor response. Science 197:165–167

    Article  PubMed  CAS  Google Scholar 

  13. Marquardt H, Philips FS, Sternberg SS (1976) Tumorigenicity in vivo and induction of malignant transformation and mutagenesis in cell cultures by adriamycin and daunomycin. Cancer Res 36:2065–2069

    PubMed  CAS  Google Scholar 

  14. Rosselli F, Zaccaro L, Venturi M, Rossi AM (1990) Persistence of drug-induced chromosome aberrations in peripheral blood lymphocytes of the rat. Mutat Res 232:107–114

    PubMed  CAS  Google Scholar 

  15. Cook NC, Samman S (1996) Flavonoids—chemistry, metabolism, cardioprotective effects, and dietary sources. J Nutr Biochem 7:66–76

    Article  CAS  Google Scholar 

  16. Jagetia GC, Jacob PS (1992) Vinblastine treatment induces dose-dependent increases in the frequency of micronuclei in mouse bone marrow. Mutat Res 280:87–92

    Article  PubMed  CAS  Google Scholar 

  17. Schmid W (1975) The micronucleus test. Mutat Res 31:9–15

    PubMed  CAS  Google Scholar 

  18. Sedlak J, Lindsay RH (1968) Estimation of total, protein-bound, and nonprotein sulfhydryl groups in tissue with Ellman’s reagent. Anal Biochem 25:192–205

    Article  PubMed  CAS  Google Scholar 

  19. Myers CE, Chabner BA (1990) Anthracyclines. In: Chabner BA, Collins JM (eds) Cancer chemotherapy: principles and practice. Lippincott, Philadelphia, Pennsylvania, pp 356–381

    Google Scholar 

  20. Rajagopalan S, Politi PM, Sinha BK, Myers CE (1988) Adriamycin-induced free radical formation in the perfused rat heart: implications for cardiotoxicity. Cancer Res 48:4766–4769

    PubMed  CAS  Google Scholar 

  21. Lee V, Randhawa AK, Singal PK (1991) Adriamycin-induced myocardial dysfunction in vitro is mediated by free radicals. Am J Physiol Heart Circ Physiol 261:H989–H995

    CAS  Google Scholar 

  22. Fantone JC, Ward PA (1982) Role of oxygen-derived free radicals and metabolites in leukocyte-dependent inflammatory reactions. Am J Pathol 107:395–418

    PubMed  CAS  Google Scholar 

  23. Fox RB (1984) Prevention of granulocyte-mediated oxidant lung injury in rats by a hydroxyl radical scavenger, dimethylthiourea. J Clin Invest 74:1456–1464

    Article  PubMed  CAS  Google Scholar 

  24. Varani J, Fligiel SE, Till GO, Kunkel RG, Ryan US, Ward PA (1985) Pulmonary endothelial cell killing by human neutrophils. Possible involvement of hydroxyl radical. Lab Invest 53:656–663

    PubMed  CAS  Google Scholar 

  25. Weiss SJ, LoBuglio AF (1982) Phagocyte-generated oxygen metabolites and cell injury. Lab Invest 47:5–18

    PubMed  CAS  Google Scholar 

  26. Morishima I, Matsui H, Mukawa H, Hayashi K, Toki Y, Okumura K, Ito T, Hayakawa T (1998) Melatonin, a pineal hormone with antioxidant property, protects against adriamycin cardiomyopathy in rats. Life Sci 63:511–521

    Article  PubMed  CAS  Google Scholar 

  27. Zbinden G, Brändle E (1975) Toxicologic screening of daunorubicin (NSC-82151), adriamycin (NSC-123127), and their derivatives in rats. Cancer Chemother Rep 59:707–715

    PubMed  CAS  Google Scholar 

  28. Sharma S, Stutzman JD, Kelloff GJ, Steele VE (1994) Screening of potential chemopreventive agents using biochemical markers of carcinogenesis. Cancer Res 54:5848–5855

    PubMed  CAS  Google Scholar 

  29. Wattenberg LW (1985) Chemoprevention of cancer. Cancer Res 45:1–8

    PubMed  CAS  Google Scholar 

  30. Devi Priya S, Shyamala Devi CS (1999) Protective effect of quercetin in cisplatin-induced cell injury in the rat kidney. Indian J Pharmacol 31:422–426

    Google Scholar 

  31. Chandrasekar MJN, Bommu P, Nanjan MJ, Suresh B (2006) Chemoprotective effect of Phyllanthus maderaspatensis in modulating cisplatin-induced nephrotoxicity and genotoxicity. Pharm Biol 44:100–106

    Article  Google Scholar 

  32. Surh Y (1999) Molecular mechanisms of chemopreventive effects of selected dietary and medicinal phenolic substances. Mutat Res 428:305–327

    PubMed  CAS  Google Scholar 

  33. Griffith OW (1999) Biologic and pharmacologic regulation of mammalian glutathione synthesis. Free Radic Biol Med 27:922–935

    Article  PubMed  CAS  Google Scholar 

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Acknowledgments

We thank Dr. Amit of Natural Remedies Pvt. Ltd., Bangalore, for providing the plant material. Praveen Bommu thanks the Department of Science and Technology, Govt. of India, New Delhi, India, for the award of a Senior Research Fellowship.

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Correspondence to Nanjan Moola Joghee.

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Bommu, P., Nanjan, C.M.J., Joghee, N.M. et al. Phyllanthus maderaspatensis, a dietary supplement for the amelioration of adriamycin-induced toxicity and oxidative stress in mice. J Nat Med 62, 149–154 (2008). https://doi.org/10.1007/s11418-007-0204-1

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